
Authors and Citation
Citation
Source: inst/CITATION
Laufer et al. Low-Pass Whole Genome Bisulfite Sequencing of Neonatal Dried Blood Spots Identifies a Role for RUNX1 in Down Syndrome DNA Methylation Profiles. Human Molecular Genetics (2020)
@Article{,
author = {Benjamin I. Laufer and Hyeyon Hwang and Julia M. Jianu and Charles E. Mordaunt and Ian F. Korf and Irva Hertz-Picciotto and Janine M. LaSalle},
title = {Low-Pass Whole Genome Bisulfite Sequencing of Neonatal Dried Blood Spots Identifies a Role for RUNX1 in Down Syndrome DNA Methylation Profiles},
journal = {Human Molecular Genetics},
year = {2020},
doi = {10.1093/hmg/ddaa218},
url = {https://doi.org/10.1101/2020.10.12.335331},
}
Korthauer et al. Detection and accurate false discovery rate control of differentially methylated regions from whole genome bisulfite sequencing. Biostatistics (2018)
@Article{,
author = {Keegan Korthauer and Sutirtha Chakraborty and Yuval Benjamini, and Rafael A Irizarry},
title = {Detection and accurate false discovery rate control of differentially methylated regions from whole genome bisulfite sequencing},
journal = {Biostatistics},
year = {2018},
doi = {10.1093/biostatistics/kxy007},
url = {https://doi.org/10.1093/biostatistics/kxy007},
}
Hansen et al. BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions. Genome Biology (2012)
@Article{,
author = {Kasper D Hansen and Benjamin Langmead and Rafael A Irizarry},
title = {BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions},
journal = {Genome Biology},
year = {2012},
doi = {10.1186/gb-2012-13-10-r83},
url = {https://doi.org/10.1186/gb-2012-13-10-r83},
}